2-(2-(1-(tert-butoxycarbonyl)piperidin-4-yl)-5-methylthiazol-4-yl)aceticacid
97%
- Product Code: 54206
CAS:
845885-88-3
| Molecular Weight: | 340.44 g./mol | Molecular Formula: | C₁₆H₂₄N₂O₄S |
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| EC Number: | MDL Number: | MFCD06656025 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research as a key intermediate in the synthesis of more complex molecules. Its structure, featuring a piperidine ring and a thiazole moiety, makes it a valuable building block for developing potential drug candidates. It is often employed in the design and synthesis of compounds targeting various biological pathways, particularly those involving enzyme inhibition or receptor modulation. Researchers leverage its functional groups to create derivatives that can be screened for therapeutic activity, such as anti-inflammatory, antiviral, or anticancer properties. Its tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthetic processes, enabling precise control over the final product's structure. This compound is particularly relevant in the development of small-molecule drugs aimed at treating complex diseases.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | £243.36 |
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2-(2-(1-(tert-butoxycarbonyl)piperidin-4-yl)-5-methylthiazol-4-yl)aceticacid
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research as a key intermediate in the synthesis of more complex molecules. Its structure, featuring a piperidine ring and a thiazole moiety, makes it a valuable building block for developing potential drug candidates. It is often employed in the design and synthesis of compounds targeting various biological pathways, particularly those involving enzyme inhibition or receptor modulation. Researchers leverage its functional groups to create derivatives that can be screened for therapeutic activity, such as anti-inflammatory, antiviral, or anticancer properties. Its tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthetic processes, enabling precise control over the final product's structure. This compound is particularly relevant in the development of small-molecule drugs aimed at treating complex diseases.
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